HemoGlide PC-2 Dialysis Catheter Kit 28cm 5664230Recalls & reported problems
Bard Access Systems, Inc. · HEMOGLIDE DIALYSIS CATH, PC, DL, 14.5 FR. 28cm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741012631), received between Jun 14, 2017 and Jun 14, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fluid/Blood Leak” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Fluid/Blood Leak1
Patient problems
- Blood Loss1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 14, 2017Fluid/Blood Leak
IT WAS REPORTED THAT THE PATIENT HAD DONE SOME PD IN THE MORNING AND WAS HAVING A 2 HOUR HD SESSION FOLLOWING HIS PD TRAINING. HE HAD BEEN DIALYZING FOR APPROXIMATELY 1 HOUR. IT WAS STATED THE HEALTHCARE PROFESSIONALS (HCPS) THEN ATTENDED TO HIS DRESSING, WHEN THEY NOTICED IT WAS LEAKING AT THE HUB, THE HCPS CEASED HD AND CLAMPED ABOVE THE SPLIT. THE HCPS ALSO NOTICED A MODERATE AMOUNT OF BLOOD ON THE PATIENT WHERE WE ASSUME IT HAD BEEN BLEEDING. THE LINE WAS REMOVED FROM THE PATIENT. NO PATIENT HARM WAS REPORTED.
Patient problems: Blood Loss
MAUDE report 6642372 ↗
Other Catheter, hemodialysis, implanted devices
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- HemoStar Long-Term Hemodialysis Catheter 5833690Bard Access Systems, Inc. · Catheter, hemodialysis, implanted2 deaths290 reports
- Palindrome 8888119369PMozarc Medical US LLC · Catheter, hemodialysis, implanted3 recalls1 death14 reports
- HemoStar Long-Term Hemodialysis Catheter 5833730Bard Access Systems, Inc. · Catheter, hemodialysis, implanted1 death141 reports
- GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet 5393230Bard Access Systems, Inc. · Catheter, hemodialysis, implanted5 deaths138 reports
- Palindrome 8888123404PMozarc Medical US LLC · Catheter, hemodialysis, implanted2 recalls1 death17 reports
- Palindrome 8888119364PMozarc Medical US LLC · Catheter, hemodialysis, implanted2 recalls1 death17 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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